ENST00000502371.3:c.3580A>T
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ENSP00000484935.2:n.3580A>T
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ENST00000504915.3:c.3969A>T
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ENSP00000473355.2:p.Ala1323=
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ENST00000505350.2:c.*3921A>T
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ENSP00000481752.1:n.*3921A>T
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ENST00000507379.6:c.3861A>T
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ENSP00000423224.2:p.Ala1287=
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ENST00000509732.6:c.3915A>T
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ENSP00000426541.2:p.Ala1305=
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ENST00000512211.7:c.3915A>T
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ENSP00000423828.3:p.Ala1305=
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ENST00000257430.9:c.3915A>T
MANE Select
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ENSP00000257430.4:p.Ala1305=
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ENST00000257430.8:c.3915A>T
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ENSP00000257430.4:p.Ala1305=
|
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ENST00000502371.2:c.2268A>T
|
|
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ENST00000508376.6:c.3915A>T
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ENSP00000427089.2:p.Ala1305=
|
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ENST00000508624.5:c.*3237A>T
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ENSP00000424265.1:n.*3237A>T
|
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ENST00000520401.1:c.230+10537A>T
|
|
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NM_000038.5:c.3915A>T
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NP_000029.2:p.Ala1305=
|
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NM_001127510.2:c.3915A>T
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NP_001120982.1:p.Ala1305=
|
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NM_001127511.2:c.3861A>T
|
NP_001120983.2:p.Ala1287=
|
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NM_001354895.1:c.3915A>T
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NP_001341824.1:p.Ala1305=
|
|
NM_001354896.1:c.3969A>T
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NP_001341825.1:p.Ala1323=
|
|
NM_001354897.1:c.3945A>T
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NP_001341826.1:p.Ala1315=
|
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NM_001354898.1:c.3840A>T
|
NP_001341827.1:p.Ala1280=
|
|
NM_001354899.1:c.3831A>T
|
NP_001341828.1:p.Ala1277=
|
|
NM_001354900.1:c.3792A>T
|
NP_001341829.1:p.Ala1264=
|
|
NM_001354901.1:c.3738A>T
|
NP_001341830.1:p.Ala1246=
|
|
NM_001354902.1:c.3642A>T
|
NP_001341831.1:p.Ala1214=
|
|
NM_001354903.1:c.3612A>T
|
NP_001341832.1:p.Ala1204=
|
|
NM_001354904.1:c.3537A>T
|
NP_001341833.1:p.Ala1179=
|
|
NM_001354905.1:c.3435A>T
|
NP_001341834.1:p.Ala1145=
|
|
NM_001354906.1:c.3066A>T
|
NP_001341835.1:p.Ala1022=
|
|
NM_000038.6:c.3915A>T
MANE Select
|
NP_000029.2:p.Ala1305=
|
|
NM_001127510.3:c.3915A>T
|
NP_001120982.1:p.Ala1305=
|
|
NM_001127511.3:c.3861A>T
|
NP_001120983.2:p.Ala1287=
|
|
NM_001354895.2:c.3915A>T
|
NP_001341824.1:p.Ala1305=
|
|
NM_001354896.2:c.3969A>T
|
NP_001341825.1:p.Ala1323=
|
|
NM_001354897.2:c.3945A>T
|
NP_001341826.1:p.Ala1315=
|
|
NM_001354898.2:c.3840A>T
|
NP_001341827.1:p.Ala1280=
|
|
NM_001354899.2:c.3831A>T
|
NP_001341828.1:p.Ala1277=
|
|
NM_001354900.2:c.3792A>T
|
NP_001341829.1:p.Ala1264=
|
|
NM_001354901.2:c.3738A>T
|
NP_001341830.1:p.Ala1246=
|
|
NM_001354902.2:c.3642A>T
|
NP_001341831.1:p.Ala1214=
|
|
NM_001354903.2:c.3612A>T
|
NP_001341832.1:p.Ala1204=
|
|
NM_001354904.2:c.3537A>T
|
NP_001341833.1:p.Ala1179=
|
|
NM_001354905.2:c.3435A>T
|
NP_001341834.1:p.Ala1145=
|
|
NM_001354906.2:c.3066A>T
|
NP_001341835.1:p.Ala1022=
|
|